Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,432 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,432 in last 12 months

Showing 5014150160 of 51,768 recalls

Medical DeviceAugust 21, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...

The Issue: During regular product monitoring, Siemens has become aware of a potential...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Remel Inc

Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the products due to a potential for false negative...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Remel Inc

Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...

The Issue: The firm is recalling the products due to a potential for false negative...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2012· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...

The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceAugust 20, 2012· Abbott Vascular

Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...

The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodAugust 18, 2012· Tanimura & Antle

Recalled Item: Tanimura & Antle Romaine Lettuce (Laitue Romaine) in plastic bag Recalled by...

The Issue: FDA was notified by CFIA of a positive result for E-cole O157:H7 in Romaine...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: Protein Shots Recalled by Protica, Inc Due to Product not sufficiently...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2012· Protica, Inc

Recalled Item: Protein Wave 15 grams of protein Recalled by Protica, Inc Due to Product not...

The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 17, 2012· Vital Signs Colorado Inc.

Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...

The Issue: There is a potential for epistaxis during use of the Disposable General...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...

The Issue: Stryker has received reports from the field indicating that certain lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...

The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2012· Haag-Streit USA Inc

Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...

The Issue: The firm recalled the device after learning of a possible deviation in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodAugust 16, 2012· J & J Snack Foods Corporation

Recalled Item: Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Recalled by J & J Snack...

The Issue: Luigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 16, 2012· Karl Storz Endoscopy America Inc

Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...

The Issue: The recall was initiated because Karl Storz has confirmed that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2012· ZOLL Medical Corporation

Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...

The Issue: Shipped with incorrect software

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 15, 2012· Hospira Inc.

Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...

The Issue: Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund